Human SNP ID | rs11158559 |
---|---|
Human chromosome | chr14 |
Human SNP position | 64774231 |
Pig chromosome | chr7 |
Pig SNP position | 95217106 |
PubMed ID | 23251661 |
---|---|
Journal | PLoS One |
Link | www.ncbi.nlm.nih.gov/pubmed/23251661 |
Study | Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population. |
Disease/Trait | Obesity-related traits |
Initial sample | 815 Hispanic children from 263 families |
Replication sample | NA |
Region | 14q23.3 |
Chromosome id | chr14 |
Chromosome position | 64774231 |
Reported gene | SPTB |
Mapped gene | SPTB |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 6710 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs11158559-A |
SNPs | rs11158559 |
Merged | 0 |
SNP id current | 11158559 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.148 |
P value | 0.000001 |
Pvalue mlog | 6 |
P value text | (Leptin ) |
Or beta | 0.03 |
%95 Ci | [NR] ng/mL increase |
Platform | Illumina [899892] |
CNV | N |
Mapped trait | leptin measurement |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0005000 |
Study accession | GCST001762 |
PubMed ID | 23251661 |
Journal | PLoS One |
Link | www.ncbi.nlm.nih.gov/pubmed/23251661 |
Study | Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population. |
Disease/Trait | Obesity-related traits |
Initial sample | 815 Hispanic children from 263 families |
Replication sample | NA |
Region | 14q23.3 |
Chromosome id | chr14 |
Chromosome position | 64774231 |
Reported gene | SPTB |
Mapped gene | SPTB |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 6710 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs11158559-A |
SNPs | rs11158559 |
Merged | 0 |
SNP id current | 11158559 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.148 |
P value | 0.000006 |
Pvalue mlog | 5.22184874961635 |
P value text | (INS ) |
Or beta | 0.03 |
%95 Ci | [NR] 碌U/mL increase |
Platform | Illumina [899892] |
CNV | N |
Mapped trait | fasting blood insulin measurement |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004466 |
Study accession | GCST001762 |